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Heart on Fire: Unmasking RyR2 Mutation in Stress-Induced Ventricular Arrhythmias Cover

Heart on Fire: Unmasking RyR2 Mutation in Stress-Induced Ventricular Arrhythmias

Open Access
|Mar 2025

References

  1. Meissner G. The structural basis of ryanodine receptor ion channel function. J Gen Physiol. 2017 Dec 4;149(12):1065-1089. doi: 10.1085/jgp.201711878
  2. Fowler ED, Zissimopoulos S. Molecular, Subcellular, and Arrhythmogenic Mechanisms in Genetic RyR2 Disease. Biomolecules. 2022 Jul 26;12(8):1030. doi: 10.3390/biom12081030
  3. Roston TM, Yuchi Z, Kannankeril PJ, et al. The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry. EP Eur. 2018 Mar 1;20(3):541-547. doi: 10.1093/europace/euw389
  4. Wleklinski MJ, Kannankeril PJ, Knollmann BC. Molecular and tissue mechanisms of catecholaminergic polymorphic ventricular tachycardia. J Physiol. 2020 Jul;598(14):2817-2834. doi: 10.1113/JP276757
  5. Szentandrássy N, Magyar , Hevesi J, Bányász T, Nánási PP, Almássy J. Therapeutic Approaches of Ryanodine Receptor-Associated Heart Diseases. Int J Mol Sci. 2022 Apr 18;23(8):4435. doi: 10.3390/ijms23084435
  6. Salvage SC, Huang CLH, Fraser JA, Dulhunty AF. How does flecainide impact RyR2 channel function? J Gen Physiol. 2022 Sep 5;154(9):e202213089. doi: 10.1085/jgp.202213089
  7. Iyer KA, Hu Y, Nayak AR, Kurebayashi N, Murayama T, Samsó M. Structural mechanism of two gain-of-function cardiac and skeletal RyR mutations at an equivalent site by cryo-EM. Sci Adv. 2020 Jul 31;6(31):eabb2964. doi: 10.1126/sciadv.abb2964
  8. Wei H, Zhang XH, Clift C, Yamaguchi N, Morad M. CRISPR/Cas9 Gene editing of RyR2 in human stem cell-derived cardiomyocytes provides a novel approach in investigating dysfunctional Ca2+ signaling. Cell Calcium. 2018 Jul;73:104-111. doi: 10.1016/j.ceca.2018.04.009
  9. Takano K, Liu D, Tarpey P, et al. An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity. Hum Mol Genet. 2012 Oct 15;21(20):4497-507. doi: 10.1093/hmg/dds292
DOI: https://doi.org/10.14797/mdcvj.1560 | Journal eISSN: 1947-6108
Language: English
Page range: 25 - 29
Submitted on: Dec 27, 2024
Accepted on: Jan 22, 2025
Published on: Mar 12, 2025
Published by: Houston Methodist DeBakey Heart & Vascular Center
In partnership with: Paradigm Publishing Services

© 2025 Vaibhav Sharma, Vishakha Maheshwari, Thirugnanasambandam Thayumanavan, Akshat Sahai, Surender Singh, Biswajit Kar, published by Houston Methodist DeBakey Heart & Vascular Center
This work is licensed under the Creative Commons Attribution-NonCommercial 4.0 License.